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We are looking for an experienced and innovative credit attorney to join our product and regulatory counsel team as Senior Counsel, reporting to the Deputy General Counsel and VP, Regulatory & Product at Robinhood.
$179,000 - $210,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our Client's FDA regulatory group works with broad range of companies, including medical devices, drugs, biologics, diagnostics, digital health, research tools, cosmetics, dietary supplements, wellness products, and other consumer products.
$150ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
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Privacy compliance strategy : Research, refine, and defend our regulatory compliance strategy; work with teams across the company to develop and implement risk mitigation plans. Transitioning to a leadership role such as General Manager, Managing Attorney, or Deputy General Counsel.
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Ensure that each group has appropriate protocols to support tech transfer including process development, QA/QC, and regulatory. Experience interacting with government regulatory agencies is a plus (FDA, DEA, etc.
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Reporting to the Director- EH&S, the Environmental Health and Safety Specialist is responsible for supporting regulatory compliance within the hospital system. Familiar with Cal OSHA, Cal EPA, Bay Area Air Quality Management District, CUPAs, fire departments and similar regulatory agencies.
$88,400 - $117,228.8 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provides quality services while meeting and maintaining familiarity with applicable rules, accreditation and regulatory issues and requirements that require Departmental, Hospital, Joint Commission, DMH, DPH, CMS, OSHA and other security-related safety standards are adhered to by assisting with problem resolution.
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Partner with the hospital manager on regulatory compliance mandates. Our state-of-the-art facility includes Anesthesiology, Cardiology, Critical Care, Dentistry, Emergency, Integrative Medicine, Internal Medicine, Neurology, Oncology, Physical Rehabilitation, Radioactive Iodine Therapy, Surgery, and Urgent Care. About the role:As an Assistant Hospital Manager in our established Emergency and Specialty hospital, you will be responsible for the following:Spend the majority of work hours on the clinic floor, interacting with and supporting all departments.
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The Manager, Regulatory Affairs will be responsible for supporting and developing global regulatory strategies for the oncology pipeline products encompassing clinical, non-clinical and CMC disciplines.
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For the health and safety of our team members and residents, Oakmont Management Group may require team members to vaccinate, participate in daily screening, surveillance testing, and to wear face coverings and other personal protective equipment (PPE) to prevent the spread of the COVID-19 or other communicable diseases, per regulatory guidelines.
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Stay up-to-date with the latest security trends, technologies, and regulatory requirements relevant to the gaming industry. Preferred: Experience in the gaming industry, familiar with game development and publishing tech stack and processesRelevant certifications such as CISSP, CEH, OSCP, or similar are highly desirable.
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The Decedent Affairs Coordinator will interact with physicians, nursing staff, Pathology Department, police, medical examiner, risk management, security, etc. The Decedent Affairs Coordinator is responsible for coordinating the care of deceased patients after a demise within Stanford Health Care and Stanford Children's Health.
$39.28 - $51.07 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Ideal candidates will also have some contentious practice experience, such as working on regulatory investigations and/or litigation, ideally focused on tech, data, privacy, cybersecurity or related issues, have experience with drafting and reviewing data processing agreements, privacy policies, and security policies, as well as providing day-to-day privacy advice to in-house counsel and start-up executives.
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Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials and other Medical Affairs activities; thorough knowledge of FDA regulations, ICH guidelines and GCPs governing the conduct of clinical trials.
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As our Senior Director, Clinical Regulatory Affairs, you’ll lead and drive Arcellx’s clinical regulatory approval strategy and implementation and oversee post-approval regulatory requirements.
$250ExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: sr Company: Csl Behring in Redwood City, CA
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